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Acetaminophen

NDC 58602-873, Acetaminophen, tablet, extended release, from Aurohealth LLC.

Product NDC
58602-873
Status
Listed
Labeler
Aurohealth LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA207229
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58602-873 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
58602-873-07586020873071 BOTTLE in 1 CARTON (58602-873-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-873-14586020873141 BOTTLE in 1 CARTON (58602-873-14) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-873-21586020873211 BOTTLE in 1 CARTON (58602-873-21) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-873-29586020873291 BOTTLE in 1 CARTON (58602-873-29) / 150 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-873-3458602087334200 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-34)
58602-873-3558602087335225 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-35)
58602-873-36586020873361 BOTTLE in 1 CARTON (58602-873-36) / 250 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-873-4058602087340500 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-40)
58602-873-41586020873411000 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-41)
58602-873-4458602087344400 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-44)
58602-873-6758602087367290 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-67)
58602-873-7658602087376325 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-76)
58602-873-9458602087394100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-873-94)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 58602-873 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58602-873 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58602-873. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.